Allele Registry

Canonical Allele Identifier: PA658668899

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000557400

RCV003227493

ClinVar Variation:

477417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1142Gln	CA8709288 NM_000334.4:c.3425G>A